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Peer-reviewed veterinary case report

Genetic variant linked to sudden heart death in young Rhodesian

By Meurs, Kathryn M et al.·Published in Genes·2019·Department of Clinical Sciences, United States·View original on PubMed

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Original publication title: A QIL1 Variant Associated with Ventricular Arrhythmias and Sudden Cardiac Death in the Juvenile Rhodesian Ridgeback Dog.

Species:
dog

Plain-English summary

A Rhodesian Ridgeback was found to have serious heart problems, including irregular heartbeats, which can lead to sudden cardiac death. Genetic testing revealed a specific mutation in a gene that affects how heart cells produce energy. This mutation was linked to the dog's arrhythmias and changes in muscle cell structure. Understanding this genetic variant can help researchers study similar heart issues in dogs and potentially improve treatments.

People also search for: Rhodesian Ridgeback heart problems · dog arrhythmia treatment · sudden cardiac death in dogs · genetic heart disease in dogs

Abstract

Thegene produces a component of the Mitochondrial Contact Site and Cristae Organizing System that forms and stabilizes mitochondrial cristae junctions and is important in cellular energy production. We previously reported a family of Rhodesian Ridgebacks with cardiac arrhythmias and sudden cardiac death. Here, we performed whole genome sequencing on a trio from the family. Variant calling was performed using a standardized bioinformatics approach. Variants were filtered against variants from 247 dogs of 43 different breeds. High impact variants were validated against additional affected and unaffected dogs. A single missense G/A variant in thegene was associated with the cardiac arrhythmia (< 0.0001). The variant was predicted to change the amino acid from conserved Glycine to Serine and to be deleterious. Ultrastructural analysis of the biceps femoris muscle from an affected dog revealed hyperplastic mitochondria, cristae rearrangement, electron dense inclusions and lipid bodies. We identified a variant in thegene resulting in a mitochondrial cardiomyopathy characterized by cristae abnormalities and cardiac arrhythmias in a canine model. This natural animal model of mitochondrial cardiomyopathy provides a large animal model with which to study the development and progression of disease as well as genotypic phenotypic relationships.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/30795627/